Pyrazolo[1,5-A]triazine corticotropin releasing factor antagonists

ABSTRACT

The present invention describes novel pyrazolo[1,5-a]triazines of formula:                    
     wherein R 3  is an alkyl, alkenyl, alkynyl, or cycloalkyl group, or pharmaceutically acceptable salt forms thereof, which are useful as CRF antagonists.

This application claims the benefit of Provisional Application No. 60/090,207, filed Jun. 22, 1998.

FIELD OF THE INVENTION

This invention relates to novel pyrazolo[1,5-a]triazines, pharmaceutical compositions containing the same and methods of using same in the treatment of psychiatric disorders and neurological diseases including affective disorder, anxiety, depression, headache, irritable bowel syndrome, post-traumatic stress disorder, supranuclear palsy, immune suppression, Alzheimer's disease, gastrointestinal diseases, anorexia nervosa or other feeding disorder, drug addiction, drug or alcohol withdrawal symptoms, inflammatory diseases, cardiovascular or heart-related diseases, fertility problems, human immunodeficiency virus infections, hemorrhagic stress, obesity, infertility, head and spinal cord traumas, epilepsy, stroke, ulcers, amyotrophic lateral sclerosis, hypoglycemia or a disorder the treatment of which can be effected or facilitated by antagonizing corticotropin releasing factor (CRF), including but not limited to disorders induced or facilitated by CRF.

BACKGROUND OF THE INVENTION

Corticotropin releasing factor, a 41 amino acid peptide, is the primary physiological regulator of proopiomelanocortin (POMC)-derived peptide secretion from the anterior pituitary gland [J. Rivier et al., Proc. Nat. Acad. Sci. (USA) 80:4851 (1983); W. Vale et al., Science 213:1394 (1981)]. In addition to its endocrine role at the pituitary gland, immunohistochemical localization of CRF has demonstrated that the hormone has a broad extrahypothalamic distribution in the central nervous system and produces a wide spectrum of autonomic, electrophysiological and behavioral effects consistent with a neurotransmitter or neuromodulator role in brain [W. Vale et al., Rec. Prog. Horm. Res. 39:245 (1983); G. F. Koob, Persp. Behav. Med. 2:39 (1985); E. B. De Souza et al., J. Neurosci. 5:3189 (1985)]. There is also evidence that CRF plays a significant role in integrating the response of the immune system to physiological, psychological, and immunological stressors [J. E. Blalock, Physiological Reviews 69:1 (1989); J. E. Morley, Life Sci. 41:527 (1987)].

Clinical data provides evidence that CRF has a role in psychiatric disorders and neurological diseases including depression, anxiety-related disorders and feeding disorders. A role for CRF has also been postulated in the etiology and pathophysiology of Alzheimer's disease, Parkinson's disease, Huntington's disease, progressive supranuclear palsy and amyotrophic lateral sclerosis as they relate to the dysfunction of CRF neurons in the central nervous system [for review see E. B. De Souza, Hosp. Practice 23:59 (1988)].

In affective disorder, or major depression, the concentration of CRF is significantly increased in the cerebral spinal fluid (CSF) of drug-free individuals [C. B. Nemeroff et al., Science 226:1342 (1984); C. M. Banki et al., Am. J. Psychiatry 144:873 (1987); R. D. France et al., Biol. Psychiatry 28:86 (1988); M. Arato et al., Biol Psychiatry 25:355 (1989)]. Furthermore, the density of CRF receptors is significantly decreased in the frontal cortex of suicide victims, consistent with a hypersecretion of CRF [C. B. Nemeroff et al., Arch. Gen. Psychiatry 45:577 (1988)]. In addition, there is a blunted adrenocorticotropin (ACTH) response to CRF (i.v. administered) observed in depressed patients [P. W. Gold et al., Am J. Psychiatry 141:619 (1984); F. Holsboer et al., Psychoneuroendocrinology 9:147 (1984); P. W. Gold et al., New Eng. J. Med. 314:1129 (1986)]. Preclinical studies in rats and non-human primates provide additional support for the hypothesis that hypersecretion of CRF may be involved in the symptoms seen in human depression [R. M. Sapolsky, Arch. Gen. Psychiatry 46:1047 (1989)]. There is preliminary evidence that tricyclic antidepressants can alter CRF levels and thus modulate the numbers of CRF receptors in brain [Grigoriadis et al., Neuropsychopharmacology 2:53 (1989)].

There has also been a role postulated for CRF in the etiology of anxiety-related disorders. CRF produces anxiogenic effects in animals and interactions between benzodiazepine/non-benzodiazepine anxiolytics and CRF have been demonstrated in a variety of behavioral anxiety models [D. R. Britton et al., Life Sci. 31:363 (1982); C. W. Berridge and A. J. Dunn Regul. Peptides 16:83 (1986)]. Preliminary studies using the putative CRF receptor antagonist α-helical ovine CRF (9-41) in a variety of behavioral paradigms demonstrate that the antagonist produces “anxiolytic-like” effects that are qualitatively similar to the benzodiazepines [C. W. Berridge and A. J. Dunn, Horm. Behav. 21:393 (1987), Brain Research Reviews 15:71 (1990)]. Neurochemical, endocrine and receptor binding studies have all demonstrated interactions between CRF and benzodiazepine anxiolytics providing further evidence for the involvement of CRF in these disorders. Chlordiazepoxide attenuates the “anxiogenic” effects of CRF in both the conflict test [K. T. Britton et al., Psychopharmacology 86:170 (1985); K. T. Britton et al., Psychopharmacology 94:306 (1988)] and in the acoustic startle test [N. R. Swerdlow et al., Psychopharmacology 88:147 (1986)] in rats. The benzodiazepine receptor antagonist (Ro15-1788), which was without behavioral activity alone in the operant conflict test, reversed the effects of CRF in a dose-dependent manner while the benzodiazepine inverse agonist (FG7142) enhanced the actions of CRF [K. T. Britton et al., Psychopharmacology 94:306 (1988)].

The mechanisms and sites of action through which the standard anxiolytics and antidepressants produce their therapeutic effects remain to be elucidated. It has been hypothesized however, that they are involved in the suppression of the CRF hypersecretion that is observed in these disorders. Of particular interest is that preliminary studies examining the effects of a CRF receptor antagonist (α-helical CRF₉₋₄₁) in a variety of behavioral paradigms have demonstrated that the CRF antagonist produces “anxiolytic-like” effects qualitatively similar to the benzodiazepines [for review see G. F. Koob and K. T. Britton, In: Corticotropin-Releasing Factor: Basic and Clinical Studies of a Neuropeptide, E. B. De Souza and C. B. Nemeroff eds., CRC Press p221 (1990)].

EP 0,778,277 (EP '277) describes a variety of CRF antagonists including those of the formula:

wherein A can be N or C, D can be N or C, E can be N or C, F can be N or C, and G can be a variety of groups. EP '277 does not disclose any pyrazolo[1,5-a]triazines.

WO 98/08847 (WO '847) describes a variety of CRF antagonists including those of the formula:

wherein A can be N or C, R⁵ is an aromatic or heteroaromatic group, and R and R³ can be a variety of groups. WO '847 does not disclose any pyrazolo[1,5-a]triazines like those of the present invention.

In view of the above, efficacious and specific antagonists of CRF are desired as potentially valuable therapeutic agents for the treatment of psychiatric disorders and neurological diseases. It is thus desirable to discover new CRF antagonists.

SUMMARY OF THE INVENTION

Accordingly, one object of the present invention is to provide novel pyrazolo[1,5-a]triazines which are useful as CRF antagonists or pharmaceutically acceptable salts or prodrugs thereof.

It is another object of the present invention to provide pharmaceutical compositions comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of at least one of the compounds of the present invention or a pharmaceutically acceptable salt form thereof.

It is another object of the present invention to provide a method for treating psychiatric disorders and neurological diseases comprising administering to a host in need of such treatment a therapeutically effective amount of at least one of the compounds of the present invention or a pharmaceutically acceptable salt form thereof.

These and other objects, which will become apparent during the following detailed description, have been achieved by the inventors' discovery that compounds of formula I:

or pharmaceutically acceptable salt forms thereof, wherein R¹, R², R³, and R⁴ are defined below, are CRF antagonists.

DETAILED DESCRIPTION OF THE INVENTION

[1] Thus, in a first embodiment, the present invention provides a novel compound of formula I:

wherein;

x is selected from N, CH and CR⁵;

R¹ is selected from H, C₁₋₄ alkyl, C₂₋₄ alkenyl, C₂₋₄ alkynyl, Cl, F, Br, I, —CN, C₁₋₄ haloalkyl, NH₂, NH(CH₃), N(CH₃)₂, NHC(O)CH₃, N(CH₃)C(O)CH₃, OH, C₁₋₄ alkoxy, SH, SCH₃, S(O)CH₃, and S(O)₂CH₃;

R² is selected from H, C₁₋₄ alkyl, C₃₋₆ cycloalkyl, Cl, F, Br, I, C₁₋₄ haloalkyl, —CN, NH(CH₃), N(CH₃)₂, NHC(O)CH₃, N(CH₃)C(O)CH₃, OH, C₁₋₄ alkoxy, SH, SCH₃, S(O)CH₃, and S(O)₂CH₃;

R³ is selected from C₁₋₁₀ alkyl substituted with 0-3 R^(a), C₂₋₁₀ alkenyl substituted with 0-3 R^(a), C₂₋₁₀ alkynyl substituted with 0-3 R^(a), C₃₋₈ cycloalkyl substituted with 0-3 R^(a), and (C₃₋₆ cycloalkyl)C₁₋₄ alkyl substituted with 0-3 R^(a);

R^(a) is independently selected at each occurrence from ═O, C₁₋₆ alkyl, C₃₋₆ cycloalkyl, Cl, F, Br, I, C₁₋₄ haloalkyl, —CN, —OR^(10a), SH, —S(O)_(n)R¹², —COR¹³, —C(O)OR¹³, —OC(O)R¹⁴, —NR⁸COR¹³, —NR⁸CONR⁶R⁷, —NR⁸C(O)OR¹², —NR⁶R⁷, —CONR⁶R⁷aryl, heteroaryl and heterocyclyl;

R⁴ is selected from H, C₁₋₄ alkyl substituted with 0-1 R^(b), allyl substituted with 0-1 R^(c), and propargyl substituted with 0-1 R^(c);

R^(b) is selected from C₃₋₆ cycloalkyl, —NR⁶R⁷, —OR¹⁰, —S(O)_(n)R¹¹ and —C(O)OR¹³;

R^(c) is selected from C₁₋₄ alkyl and C₃₋₆ cycloalkyl;

R⁵ is independently selected at each occurrence from C₁₋₆ alkyl substituted with 0-2 R^(d), C₂₋₆ alkenyl substituted with 0-2 R^(d), C₂₋₆ alkynyl substituted with 0-2 R^(d), C₃₋₆ cycloalkyl substituted with 0-2 R^(d), (C₃₋₆ cycloalkyl)C₁₋₄ alkyl substituted with 0-2 R^(d), —NO₂, Cl, F, Br, I, —CN, C₁₋₄ haloalkyl, —NR⁶R⁷, —NR⁸COR¹³, —NR⁸C(O)OR¹², —COR¹³, —OR¹⁰, —CONR⁶R⁷, —NR⁸CONR⁶R⁷, —C(O)OR¹⁰, SH, and —S(O)_(n)R¹²;

R^(d) is independently selected at each occurrence from C₁₋₄ alkyl, —NO₂, Cl, F, Br, I, —CN, —NR⁶R⁷, —NR⁸COR¹³, —NR⁸C(O)OR¹², —COR¹³, —OR¹⁰, —CONR⁶R⁷, —NR⁸CONR⁶R⁷, —C(O)OR¹⁰, SH, and —S(O)_(n)R¹²;

R⁶ is independently selected at each occurrence from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)methyl, and C₁₋₄ haloalkyl;

R⁷ is independently selected at each occurrence from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)methyl, and C₁₋₄ haloalkyl;

alternatively, NR⁶R⁷ is selected from piperidine, pyrrolidine, morpholine, thiomorpholine, thiomorpholine-oxide, and thiomorpholine-dioxide, and is substituted with 0-1 R^(e);

R^(e) is C₁₋₄ alkyl;

alternatively, NR⁶R⁷ is piperazine substituted on the nitrogen with 0-1 R^(f) and substituted on a carbon with 0-1 R^(e);

R^(f) is selected from C₁₋₄ alkyl, C(O)C₁₋₄ alkyl, C(O)benzyl, C(O)OC₁₋₄ alkyl, C(O)O-benzyl, SO₂—C₁₋₄ alkyl, SO₂-benzyl, and SO₂-phenyl;

R⁸ is independently at each occurrence selected from H, C₁₋₄ alkyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, and benzyl;

R¹⁰ is independently selected at each occurrence from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, C₁₋₄ hydroxyalkyl, C₁₋₄ haloalkyl, (NR⁶R⁷)C₁₋₄ alkyl, (C₁₋₄ alkyl)₂-amino-C₁₋₄ alkyl, and SO₂—C₁₋₄ alkyl;

R^(10a) is independently selected at each occurrence from H, C₁₋₆ alkyl, C₂₋₄ alkenyl, phenyl, benzyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, and C₁₋₄ haloalkyl;

R¹¹ is independently at each occurrence selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl, and C₃₋₆ cycloalkyl;

R¹² is independently at each occurrence selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, aryl, and (aryl)C₁₋₄ alkyl;

R¹³ is independently at each occurrence selected from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, and (C₃₋₆ cycloalkyl)C₁₋₄ alkyl;

R¹⁴ is independently at each occurrence selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, aryl, and (aryl)C₁₋₄ alkyl;

aryl is independently at each occurrence selected from phenyl and naphthyl, and is substituted with 0-3 R^(g);

R^(g) is independently at each occurrence selected from C₁₋₆ alkyl, C₃₋₆ cycloalkyl, Cl, F, Br, I, C₁₋₄ haloalkyl, cyano, nitro, —OR¹⁰, SH, —S(O)_(n)R¹⁵, —COR¹⁶, —C(O)OR¹⁶, —OC(O)R¹⁷, —NR⁸COR¹⁶, —NR⁸CONR⁶R⁷, —NR⁸C(O)OR¹², —NR⁶R⁷, and —CONR⁶R⁷;

R¹⁵ is independently at each occurrence selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, phenyl, benzyl, and (phenyl)C₁₋₄ alkyl;

R¹⁶ is independently at each occurrence selected from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, and (C₃₋₆ cycloalkyl)C₁₋₄ alkyl;

R¹⁷ is independently at each occurrence selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, phenyl, benzyl, (phenyl)C₁₋₄ alkyl, heteroaryl and (heteroaryl)C₁₋₄ alkyl;

heteroaryl is independently at each occurrence selected from pyridyl, pyrimidinyl, triazinyl, furanyl, quinolinyl, isoquinolinyl, thienyl, imidazolyl, thiazolyl, indolyl, pyrrolyl, oxazolyl, benzofuranyl, benzothienyl, benzthiazolyl, isoxazolyl, pyrazolyl, triazolyl, tetrazolyl, and indazolyl, and is substituted with 0-3 R^(h);

heterocyclyl is saturated or partially saturated heteroaryl, substituted with 0-3 R^(h); and

R^(h) is independently at each occurrence selected from C₁₋₆ alkyl, C₃₋₆ cycloalkyl, Cl, F, Br, I, C₁₋₄ haloalkyl, cyano, nitro, —OR¹⁰, SH, —S(O)_(n)R¹⁵ —COR¹⁶, —C(O)OR¹⁶, —OC(O)R¹⁸, —NR⁸COR¹⁶, —NR⁸CONR⁶R⁷, —NR⁸C(O)OR¹², —NR⁶R⁷, and —CONR⁶R⁷;

R¹⁸ is independently selected at each occurrence from C₁₋₆ alkyl, C₃₋₆ cycloalkyl, phenyl and benzyl;

n is independently at each occurrence selected from 0, 1 and 2; and,

r is selected from 0, 1, 2, 3, and 4.

[2] In a preferred embodiment, the present invention provides novel compounds, wherein:

R¹ is selected from H, CH₃, CH₂CH₃, Cl, F, Br, —CN, CF₃, NH₂, NH(CH₃), N(CH₃)₂, OH, OCH₃, SH, SCH₃, and S(O)₂CH₃;

R² is selected from H, CH₃, CH₂CH₃, Cl, F, Br, —CN, CF₃, NH(CH₃), N(CH₃)₂, OH, OCH₃, SH, SCH₃, and S(O)₂CH₃;

R³ is selected from C₁₋₆ alkyl substituted with 0-2 R^(a), C₂₋₆ alkenyl substituted with 0-2 R^(a), and C₂₋₆ alkynyl substituted with 0-2 R^(a);

R^(a) is independently selected at each occurrence from ═O, CH₃, CH₂CH₃, cyclopropyl, cyclopentyl, cyclohexyl, Cl, F, Br, CF₃, —CN, —OH, OCH₃, OCH₂CH₃, SH, —S(O)_(n)R¹² —COR¹³, —C(O)OR¹³, —NR⁸COR¹³, —NR⁶R⁷, —CONR⁶R⁷, aryl, heteroaryl and heterocyclyl;

R⁴ is selected from H, CH₃, CH₂CH₃;

R⁵ is independently selected at each occurrence from CH₃, CH₂CH₃, cyclopropyl, cyclopentyl, cyclohexyl, Cl, F, Br, —CN, CF₃, —NR⁶R⁷, COR¹³, —OR¹⁰, —CONR⁶R⁷, —C(O)OR¹⁰, SH, and —S(O)_(n)R¹²;

R⁶ is independently selected at each occurrence from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)methyl, and C₁₋₄ haloalkyl;

R⁷ is independently selected at each occurrence from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)methyl, and C₁₋₄ haloalkyl;

alternatively, NR⁶R⁷ is selected from piperidine, pyrrolidine, morpholine, thiomorpholine, thiomorpholine-oxide, and thiomorpholine-dioxide, and is substituted with 0-1 R^(e);

R^(e) is CH₃;

alternatively, NR⁶R⁷ is piperazine substituted on the nitrogen with 0-1 R^(f) and substituted on a carbon with 0-1 R^(e);

R^(f) is selected from CH₃, C(O)CH₃, C(O)benzyl, CO₂CH₃, CO₂-benzyl, SO₂CH₃, SO₂-benzyl, and SO₂-phenyl;

R⁸ is independently at each occurrence selected from H and C₁₋₄ alkyl;

R¹⁰ is independently selected at each occurrence from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, C₁₋₄ hydroxyalkyl, C₁₋₄ haloalkyl, (NR⁶R⁷)C₁₋₄ alkyl, (C₁₋₄ alkyl)₂-amino-C₁₋₄ alkyl, and SO₂—C₁₋₄ alkyl;

R¹² is independently at each occurrence selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, aryl, and (aryl) C₁₋₄ alkyl;

R¹³ is independently at each occurrence selected from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, and (C₃₋₆ cycloalkyl)C₁₋₄ alkyl;

aryl is independently at each occurrence selected from phenyl and naphthyl, and is substituted with 0-3 R^(g);

R^(g) is independently at each occurrence selected from C₁₋₆ alkyl, C₃₋₆ cycloalkyl, Cl, F, Br, I, C₁₋₄ haloalkyl, cyano, nitro, —OR¹⁰, SH, —S(O)_(n)R¹⁵, —COR¹⁶, —C(O)OR¹⁶, —OC(O)R¹⁷, —NR⁸COR¹⁶, —NR⁸CONR⁶R⁷, —NR⁸C(O)OR¹², —NR⁶R⁷, and —CONR⁶R⁷;

R¹⁵ is independently at each occurrence selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, phenyl, benzyl, and (phenyl)C₁₋₄ alkyl;

R¹⁶ is independently at each occurrence selected from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, and (C₃₋₆ cycloalkyl)C₁₋₄ alkyl;

R¹⁷ is independently at each occurrence selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, phenyl, benzyl, (phenyl)C₁₋₄ alkyl, heteroaryl and (heteroaryl)C₁₋₄ alkyl;

heteroaryl is independently at each occurrence selected from pyridyl, pyrimidinyl, triazinyl, furanyl, quinolinyl, isoquinolinyl, thienyl, imidazolyl, thiazolyl, indolyl, pyrrolyl, oxazolyl, benzofuranyl, benzothienyl, benzthiazolyl, isoxazolyl, pyrazolyl, triazolyl, tetrazolyl, and indazolyl, and is substituted with 0-3 R^(h);

heterocyclyl is saturated or partially saturated heteroaryl, substituted with 0-3 R^(h); and

R^(h) is independently at each occurrence selected from CH₃, CH₂CH₃, cyclopropyl, cyclopentyl, cyclohexyl, Cl, F, Br, CF₃, —CN, nitro, —OR¹⁰, SH, —S(O)_(n)R¹⁵, —COR¹⁶, —C(O)OR¹⁶, —NR⁶R⁷, and —CONR⁶R⁷;

n is independently at each occurrence selected from 0, 1 and 2; and,

r is selected from 0, 1, 2, 3, and 4.

[3] In a more preferred embodiment, the present invention provides novel compounds, wherein:

R¹ is selected from H, CH₃, CH₂CH₃, Cl, and F;

R² is selected from H, CH₃, CH₂CH₃, Cl and F;

R³ is selected from C₁₋₆ alkyl substituted with 0-2 R^(a), C₂₋₆ alkenyl substituted with 0-2 R^(a), and C₂₋₆ alkynyl substituted with 0-2 R^(a);

R^(a) is independently selected at each occurrence from CH₃, CH₂CH₃, cyclopropyl, cyclopentyl, cyclohexyl, Cl, F, Br, CF₃, —CN, —OH, OCH₃, and OCH₂CH₃;

R⁴ is selected from H, CH₃, CH₂CH₃;

R⁵ is independently selected at each occurrence from CH₃, CH₂CH₃, CH(CH₃)₂, cyclopropyl, cyclopentyl, cyclohexyl, Cl, F, Br, —CN, CF₃, —NR⁶R⁷, OCH₃, OCH₂CH₃, SCH₃, SOCH₃, and SO₂CH₃;

R⁶ is independently selected at each occurrence from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)methyl, and C₁₋₄ haloalkyl;

R⁷ is independently selected at each occurrence from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)methyl, and C₁₋₄ haloalkyl;

alternatively, NR⁶R⁷ is selected from piperidine, pyrrolidine, morpholine, thiomorpholine, thiomorpholine-oxide, and thiomorpholine-dioxide, and is substituted with 0-1 R^(e);

R^(e) is CH₃;

alternatively, NR⁶R⁷ is piperazine substituted on the nitrogen with 0-1 R^(f) and substituted on a carbon with 0-1 R^(e);

R^(f) is selected from CH₃, CH₂CH₃, C(O)CH₃, CO₂CH₃, SO₂CH₃, and CO₂-benzyl; and,

r is selected from 1, 2, and 3.

[4] In an even more preferred embodiment, the present invention provides novel compounds, wherein:

R¹ is CH₃;

R² is selected from H and CH₃;

R³ is selected from 2-propyl, 2-butyl, 2-pentyl, 3-pentyl, trans-pent-2-en-4-yl, pent-2-yn-4-yl, 3-hexyl, hex-1-en-3-yl, hex-2-yn-4-yl, 1-(cyclopropyl)ethyl, 1-(cyclopropyl)propyl, 3-(cyclopropyl)prop-1-en-3-yl, 1-(cyclopropyl)butyl, dicyclopropylmethyl, 1-(cyclopropyl)but-2-yn-1-yl, trans-1-(cyclopropyl)but-2-en-1-yl, 1-(cyclobutyl)ethyl, 1-(cyclobutyl)propyl, 1-(cyclobutyl)butyl, 1-(cyclopropyl)but-2-yn-1-yl, dicyclobutylmethyl, cyclopentyl, 1-methoxyprop-2-yl, 1-methoxybut-2-yl, 1,3-dimethoxyprop-2-yl, 1,4-dimethoxybut-2-yl, and 1-cyclopropyl-2-methoxyethyl;

R⁴ is selected from H, CH₃, and CH₂CH₃;

R⁵ is independently selected at each occurrence from CH₃, CH₂CH₃, CH(CH₃)₂, cyclopropyl, cyclopentyl, cyclohexyl, Cl, F, Br, —CN, CF₃, —NR⁶R⁷, OCH₃, OCH₂CH₃, SCH₃, SOCH₃, and SO₂CH₃;

R⁶ is independently selected at each occurrence from H, CH₃, CH₂CH₃, phenyl, benzyl, cyclopropyl, cyclopentyl, cyclohexyl, cyclopropylmethyl, cyclopentylmethyl, cyclohexylmethyl, and CF₃;

R⁷ is independently selected at each occurrence from H, CH₃, CH₂CH₃, phenyl, benzyl, cyclopropyl, cyclopentyl, cyclohexyl, cyclopropylmethyl, cyclopentylmethyl, cyclohexylmethyl, and CF₃;

alternatively, NR⁶R⁷ is selected from piperidine, pyrrolidine, morpholine, thiomorpholine, thiomorpholine-oxide, and thiomorpholine-dioxide, and is substituted with 0-1 R^(e);

R^(e) is CH₃;

alternatively, NR⁶R⁷ is piperazine substituted on the nitrogen with 0-1 R^(f) and substituted on a carbon with 0-1 R^(e);

R^(f) is selected from CH₃, CH₂CH₃, C(O)CH₃, CO₂CH₃, SO₂CH₃, and CO₂-benzyl; and,

r is selected from 1, 2, and 3.

[5] In a further preferred embodiment, the present invention provides a compound selected from the group:

8-(3-Pentyl)-2-methyl-4-(2,4,6-trimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(3-Pentyl)-2-methyl-4-(2-chloro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(3-Pentyl)-2-methyl-4-(4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(3-Pentyl)-2-methyl-4-(2,4-dichlorophenyl)aminopyrazolo[1,5-a]triazine;

8-(3-Pentyl)-2-methyl-4-(2-chloro-4-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(3-Pentyl)-2-methyl-4-(4-chloro-2-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(3-Pentyl)-2-methyl-4-(2,4,6-trichlorophenyl)aminopyrazolo[1,5-a]triazine;

8-(3-Pentyl)-2-methyl-4-(2,6-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(3-Pentyl)-2-methyl-4-(2-methyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(3-Pentyl)-2-methyl-4-(2,5-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(3-Pentyl)-2-methyl-4-(2-chloro-5-fluoro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(3-Pentyl)-2-methyl-4-(4,6-dimethyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(3-Pentyl)-2-methyl-4-(2,4-dichloro-6-methylphenyl)aminopyrazolo[1,5-a]triazine;

8-(3-Pentyl)-2-methyl-4-(4-methyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(3-Pentyl)-2-methyl-4-(2-dimethylamino-4-methylpyrid-3-yl)aminopyrazolo[1,5-a]triazine;

8-(1-Methoxybut-2-yl)-2-methyl-4-(2,4,6-trimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Methoxybut-2-yl)-2-methyl-4-(2-chloro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Methoxybut-2-yl)-2-methyl-4-(4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Methoxybut-2-yl)-2-methyl-4-(2,4-dichlorophenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Methoxybut-2-yl)-2-methyl-4-(2-chloro-4-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Methoxybut-2-yl)-2-methyl-4-(4-chloro-2-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Methoxybut-2-yl)-2-methyl-4-(2,4,6-trichlorophenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Methoxybut-2-yl)-2-methyl-4-(2,6-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Methoxybut-2-yl)-2-methyl-4-(2-methyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Methoxybut-2-yl)-2-methyl-4-(2,5-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Methoxybut-2-yl)-2-methyl-4-(2-chloro-5-fluoro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Methoxybut-2-yl)-2-methyl-4-(4,6-dimethyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Methoxybut-2-yl)-2-methyl-4-(2,4-dichloro-6-methylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Methoxybut-2-yl)-2-methyl-4-(4-methyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Methoxybut-2-yl)-2-methyl-4-(2-dimethylamino-4-methylpyrid-3-yl)aminopyrazolo[1,5-a]triazine;

8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2,4,6-trimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2-chloro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2,4-dichlorophenyl)aminopyrazolo[1,5-a]triazine;

8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2-chloro-4-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(4-chloro-2-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2,4,6-trichlorophenyl)aminopyrazolo[1,5-a]triazine;

8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2,6-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2-methyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2,5-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2-chloro-5-fluoro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(4,6-dimethyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2,4-dichloro-6-methylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(4-methyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2-dimethylamino-4-methylpyrid-3-yl)aminopyrazolo[1,5-a]triazine;

8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2,4,6-trimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2-chloro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2,4-dichlorophenyl)aminopyrazolo[1,5-a]triazine;

8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2-chloro-4-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(4-chloro-2-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2,4,6-trichlorophenyl)aminopyrazolo[1,5-a]triazine;

8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2,6-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2-methyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2,5-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2-chloro-5-fluoro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(4,6-dimethyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2,4-dichloro-6-methylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(4-methyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2-dimethylamino-4-methylpyrid-3-yl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)propyl-2-methyl-4-(2,4,6-trimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)propyl-2-methyl-4-(2-chloro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)propyl-2-methyl-4-(4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)propyl-2-methyl-4-(2,4-dichlorophenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)propyl-2-methyl-4-(2-chloro-4-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)propyl-2-methyl-4-(4-chloro-2-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)propyl-2-methyl-4-(2,4,6-trichlorophenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)propyl-2-methyl-4-(2,6-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)propyl-2-methyl-4-(2-methyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)propyl-2-methyl-4-(2,5-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)propyl-2-methyl-4-(2-chloro-5-fluoro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)propyl-2-methyl-4-(4,6-dimethyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)propyl-2-methyl-4-(2,4-dichloro-6-methylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)propyl-2-methyl-4-(4-methyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)propyl-2-methyl-4-(2-dimethylamino-4-methylpyrid-3-yl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)butyl-2-methyl-4-(2,4,6-trimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)butyl-2-methyl-4-(2-chloro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)butyl-2-methyl-4-(4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)butyl-2-methyl-4-(2,4-dichlorophenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)butyl-2-methyl-4-(2-chloro-4-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)butyl-2-methyl-4-(4-chloro-2-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)butyl-2-methyl-4-(2,4,6-trichlorophenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)butyl-2-methyl-4-(2,6-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)butyl-2-methyl-4-(2-methyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)butyl-2-methyl-4-(2,5-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)butyl-2-methyl-4-(2-chloro-5-fluoro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)butyl-2-methyl-4-(4,6-dimethyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)butyl-2-methyl-4-(2,4-dichloro-6-methylphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)butyl-2-methyl-4-(4-methyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(1-Cyclopropyl)butyl-2-methyl-4-(2-dimethylamino-4-methylpyrid-3-yl)aminopyrazolo[1,5-a]triazine;

8-(2-Pentyl)-2-methyl-4-(2,4,6-trimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(2-Pentyl)-2-methyl-4-(2-chloro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(2-Pentyl)-2-methyl-4-(4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(2-Pentyl)-2-methyl-4-(2,4-dichlorophenyl)aminopyrazolo[1,5-a]triazine;

8-(2-Pentyl)-2-methyl-4-(2-chloro-4-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(2-Pentyl)-2-methyl-4-(4-chloro-2-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(2-Pentyl)-2-methyl-4-(2,4,6-trichlorophenyl)aminopyrazolo[1,5-a]triazine;

8-(2-Pentyl)-2-methyl-4-(2,6-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(2-Pentyl)-2-methyl-4-(2-methyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(2-Pentyl)-2-methyl-4-(2,5-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(2-Pentyl)-2-methyl-4-(2-chloro-5-fluoro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine;

8-(2-Pentyl)-2-methyl-4-(4,6-dimethyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine;

8-(2-Pentyl)-2-methyl-4-(2,4-dichloro-6-methylphenyl)aminopyrazolo[1,5-a]triazine;

8-(2-Pentyl)-2-methyl-4-(4-methyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine; and,

8-(2-Pentyl)-2-methyl-4-(2-dimethylamino-4-methylpyrid-3-yl)aminopyrazolo[1,5-a]triazine;

or a pharmaceutically acceptable salt form thereof.

In another embodiment, the present invention provides pharmaceutical compositions comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of at least one of the compounds of the present invention or a pharmaceutically acceptable salt form thereof.

In another embodiment, the present invention provides a method of treating psychiatric disorders and neurological diseases including affective disorder, anxiety, depression, headache, irritable bowel syndrome, post-traumatic stress disorder, supranuclear palsy, immune suppression, Alzheimer's disease, gastrointestinal diseases, anorexia nervosa or other feeding disorder, drug addiction, drug or alcohol withdrawal symptoms, inflammatory diseases, cardiovascular or heart-related diseases, fertility problems, human immunodeficiency virus infections, hemorrhagic stress, obesity, infertility, head and spinal cord traumas, epilepsy, stroke, ulcers, amyotrophic lateral sclerosis, hypoglycemia or a disorder the treatment of which can be effected or facilitated by antagonizing CRF, including but not limited to disorders induced or facilitated by CRF, in a mammal, comprising: administering to the mammal a therapeutically effective amount of a compound of formula (I) or a pharmaceutically acceptable salt form thereof.

In another embodiment, the present invention provides intermediate compounds useful in preparation of the CRF antagonist compounds and processes for making those intermediates, as described in the following description and claims.

The CRF antagonist compounds provided by this invention and labelled derivatives thereof are also useful as standards and reagents in determining the ability of a potential pharmaceutical to bind to the CRF receptor.

Definitions

The compounds herein described may have asymmetric centers. Compounds of the present invention containing an asymmetrically substituted atom may be isolated in optically active or racemic forms. It is well known in the art how to prepare optically active forms, such as by resolution of racemic forms or by synthesis from optically active starting materials. Many geometric isomers of olefins, C═N double bonds, and the like can also be present in the compounds described herein, and all such stable isomers are contemplated in the present invention. Cis and trans geometric isomers of the compounds of the present invention are described and may be isolated as a mixture of isomers or as separated isomeric forms. All chiral, diastereomeric, racemic forms and all geometric isomeric forms of a structure are intended, unless the specific stereochemistry or isomeric form is specifically indicated.

The term “substituted,” as used herein, means that any one or more hydrogens on the designated atom is replaced with a selection from the indicated group, provided that the designated atom's normal valency is not exceeded, and that the substitution results in a stable compound. When a substitent is keto (i.e., ═O), then 2 hydrogens on the atom are replaced. Keto substituents are not present on aromatic moieties.

The present invention is intended to include all isotopes of atoms occurring in the present compounds. Isotopes include those atoms having the same atomic number but different mass numbers. By way of general example and without limitation, isotopes of hydrogen include tritium and deuterium. Isotopes of carbon include C-13 and C-14.

When any variable (e.g., R⁶) occurs more than one time in any constituent or formula for a compound, its definition at each occurrence is independent of its definition at every other occurrence. Thus, for example, if a group is shown to be substituted with 0-2 R⁶, then said group may optionally be substituted with up to two R⁶ groups and R⁶ at each occurrence is selected independently from the definition of R⁶. Also, combinations of substituents and/or variables are permissible only if such combinations result in stable compounds.

When a bond to a substituent is shown to cross a bond connecting two atoms in a ring, then such substituent may be bonded to any atom on the ring. When a substituent is listed without indicating the atom via which such substituent is bonded to the rest of the compound of a given formula, then such substituent may be bonded via any atom in such substituent. Combinations of substituents and/or variables are permissible only if such combinations result in stable compounds.

As used herein, “alkyl” is intended to include both branched and straight-chain saturated aliphatic hydrocarbon groups having the specified number of carbon atoms. Examples of alkyl include, but are not limited to, methyl, ethyl, n-propyl, i-propyl, n-butyl, s-butyl, t-butyl, n-pentyl, and s-pentyl. “Haloalkyl” is intended to include both branched and straight-chain saturated aliphatic hydrocarbon groups having the specified number of carbon atoms, substituted with 1 or more halogen (for example —C_(v)F_(w) where v=1 to 3 and w=1 to (2v+1)). Examples of haloalkyl include, but are not limited to, trifluoromethyl, trichloromethyl, pentafluoroethyl, and pentachloroethyl. “Alkoxy” represents an alkyl group as defined above with the indicated number of carbon atoms attached through an oxygen bridge. Examples of alkoxy include, but are not limited to, methoxy, ethoxy, n-propoxy, i-propoxy, n-butoxy, s-butoxy, t-butoxy, n-pentoxy, and s-pentoxy. “Cycloalkyl” is intended to include saturated ring groups, such as cyclopropyl, cyclobutyl, or cyclopentyl. Alkenyl” is intended to include hydrocarbon chains of either a straight or branched configuration and one or more unsaturated carbon-carbon bonds which may occur in any stable point along the chain, such as ethenyl and propenyl. “Alkynyl” is intended to include hydrocarbon chains of either a straight or branched configuration and one or more triple carbon-carbon bonds which may occur in any stable point along the chain, such as ethynyl and propynyl.

“Halo” or “halogen” as used herein refers to fluoro, chloro, bromo, and iodo; and “counter-ion” is used to represent a small, negatively charged species such as chloride, bromide, hydroxide, acetate, sulfate, and the like.

As used herein, “carbocycle” or “carbocyclic residue” is intended to mean any stable 3- to 7-membered monocyclic or bicyclic or 7- to 13-membered bicyclic or tricyclic, any of which may be saturated, partially unsaturated, or aromatic. Examples of such carbocycles include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, adamantyl, cyclooctyl, [3.3.0]bicyclooctane, [4.3.0]bicyclononane, [4.4.0]bicyclodecane, [2.2.2]bicyclooctane, fluorenyl, phenyl, naphthyl, indanyl, adamantyl, and tetrahydronaphthyl.

As used herein, the term “heterocycle” or “heterocyclic system” is intended to mean a stable 5- to 7-membered monocyclic or bicyclic or 7- to 10-membered bicyclic heterocyclic ring which is saturated partially unsaturated or unsaturated (aromatic), and which consists of carbon atoms and from 1 to 4 heteroatoms independently selected from the group consisting of N, O and S and including any bicyclic group in which any of the above-defined heterocyclic rings is fused to a benzene ring. The nitrogen and sulfur heteroatoms may optionally be oxidized. The heterocyclic ring may be attached to its pendant group at any heteroatom or carbon atom which results in a stable structure. The heterocyclic rings described herein may be substituted on carbon or on a nitrogen atom if the resulting compound is stable. A nitrogen in the heterocycle may optionally be quaternized. It is preferred that when the total number of S and O atoms in the heterocycle exceeds 1, then these heteroatoms are not adjacent to one another. It is preferred that the total number of S and O atoms in the heterocycle is not more than 1. As used herein, the term “aromatic heterocyclic system” is intended to mean a stable 5- to 7-membered monocyclic or bicyclic or 7- to 10-membered bicyclic heterocyclic aromatic ring which consists of carbon atoms and from 1 to 4 heterotams independently selected from the group consisting of N, O and S. It is preferred that the total number of S and O atoms in the aromatic heterocycle is not more than 1.

Examples of heterocycles include, but are not limited to, acridinyl, azocinyl, benzimidazolyl, benzofuranyl, benzothiofuranyl, benzothiophenyl, benzoxazolyl, benzthiazolyl, benztriazolyl, benztetrazolyl, benzisoxazolyl, benzisothiazolyl, benzimidazolinyl, carbazolyl, 4aH-carbazolyl, carbolinyl, chromanyl, chromenyl, cinnolinyl, decahydroquinolinyl, 2H, 6H-1,5,2-dithiazinyl, dihydrofuro[2,3-b]tetrahydrofuran, furanyl, furazanyl, imidazolidinyl, imidazolinyl, imidazolyl, 1H-indazolyl, indolenyl, indolinyl, indolizinyl, indolyl, 3H-indolyl, isobenzofuranyl, isochromanyl, isoindazolyl, isoindolinyl, isoindolyl, isoquinolinyl, isothiazolyl, isoxazolyl, morpholinyl, naphthyridinyl, octahydroisoquinolinyl, oxadiazolyl, 1,2,3-oxadiazolyl, 1,2,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,3,4-oxadiazolyl, oxazolidinyl, oxazolyl, oxazolidinyl, pyrimidinyl, phenanthridinyl, phenanthrolinyl, phenazinyl, phenothiazinyl, phenoxathiinyl, phenoxazinyl, phthalazinyl, piperazinyl, piperidinyl, pteridinyl, purinyl, pyranyl, pyrazinyl, pyrazolidinyl, pyrazolinyl, pyrazolyl, pyridazinyl, pyridooxazole, pyridoimidazole, pyridothiazole, pyridinyl, pyridyl, pyrimidinyl, pyrrolidinyl, pyrrolinyl, 2H-pyrrolyl, pyrrolyl, quinazolinyl, quinolinyl, 4H-quinolizinyl, quinoxalinyl, quinuclidinyl, tetrahydrofuranyl, tetrahydroisoquinolinyl, tetrahydroquinolinyl, 6H-1,2,5-thiadiazinyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,2,5-thiadiazolyl, 1,3,4-thiadiazolyl, thianthrenyl, thiazolyl, thienyl, thienothiazolyl, thienooxazolyl, thienoimidazolyl, thiophenyl, triazinyl, 1,2,3-triazolyl, 1,2,4-triazolyl, 1,2,5-triazolyl, 1,3,4-triazolyl, and xanthenyl. Preferred heterocycles include, but are not limited to, pyridinyl, furanyl, thienyl, pyrrolyl, pyrazolyl, pyrrolidinyl, imidazolyl, indolyl, benzimidazolyl, 1H-indazolyl, oxazolidinyl, benzotriazolyl, benzisoxazolyl, oxindolyl, benzoxazolinyl, and isatinoyl. Also included are fused ring and spiro compounds containing, for example, the above heterocycles.

The phrase “pharmaceutically acceptable” is employed herein to refer to those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.

As used herein, “pharmaceutically acceptable salts” refer to derivatives of the disclosed compounds wherein the parent compound is modified by making acid or base salts thereof. Examples of pharmaceutically acceptable salts include, but are not limited to, mineral or organic acid salts of basic residues such as amines; alkali or organic salts of acidic residues such as carboxylic acids; and the like. The pharmaceutically acceptable salts include the conventional non-toxic salts or the quaternary ammonium salts of the parent compound formed, for example, from non-toxic inorganic or organic acids. For example, such conventional non-toxic salts include those derived from inorganic acids such as hydrochloric, hydrobromic, sulfuric, sulfamic, phosphoric, nitric and the like; and the salts prepared from organic acids such as acetic, propionic, succinic, glycolic, stearic, lactic, malic, tartaric, citric, ascorbic, pamoic, maleic, hydroxymaleic, phenylacetic, glutamic, benzoic, salicylic, sulfanilic, 2-acetoxybenzoic, fumaric, toluenesulfonic, methanesulfonic, ethane disulfonic, oxalic, isethionic, and the like.

The pharmaceutically acceptable salts of the present invention can be synthesized from the parent compound which contains a basic or acidic moiety by conventional chemical methods. Generally, such salts can be prepared by reacting the free acid or base forms of these compounds with a stoichiometric amount of the appropriate base or acid in water or in an organic solvent, or in a mixture of the two; generally, nonaqueous media like ether, ethyl acetate, ethanol, isopropanol, or acetonitrile are preferred. Lists of suitable salts are found in Remington's Pharmaceutical Sciences, 17th ed., Mack Publishing Company, Easton, Pa., 1985, p. 1418, the disclosure of which is hereby incorporated by reference.

“Prodrugs” are intended to include any covalently bonded carriers which release the active parent drug according to formula (I) in vivo when such prodrug is administered to a mammalian subject. Prodrugs of a compound of formula (I) are prepared by modifying functional groups present in the compound in such a way that the modifications are cleaved, either in routine manipulation or in vivo, to the parent compound. Prodrugs include compounds of formula (I) wherein a hydroxy, amino, or sulfhydryl group is bonded to any group that, when the prodrug or compound of formula (I) is administered to a mammalian subject, cleaves to form a free hydroxyl, free amino, or free sulfhydryl group, respectively. Examples of prodrugs include, but are not limited to, acetate, formate and benzoate derivatives of alcohol and amine functional groups in the compounds of formula (I), and the like.

Combinations of substituents and/or variables are permissible only if such combinations result in stable compounds. A stable compound or stable structure is meant to imply a compound that is sufficiently robust to survive isolation to a useful degree of purity from a reaction mixture, and formulation into an effective therapeutic agent.

The term “therapeutically effective amount” of a compound of this invention means an amount effective to antagonize abnormal level of CRF or treat the symptoms of affective disorder, anxiety or depression in a host.

Synthesis

The compounds of the present invention can be prepared in a number of ways well known to one skilled in the art of organic synthesis. The compounds of the present invention can be synthesized using the methods described below, together with synthetic methods known in the art of synthetic organic chemistry, or variations thereon as appreciated by those skilled in the art. Preferred methods include but are not limited to those methods described below. Each of the references cited below are hereby incorporated herein by reference.

The compounds of the present invention can be synthesized using the methods described below, together with synthetic methods known in the art of synthetic organic chemistry, or variations thereon as appreciated by those skilled in the art. Preferred methods include, but are not limited to, those described below. All references cited herein are hereby incorporated in their entirety herein by reference.

The following abbreviations are used herein:

AcOH acetic acid DMF N,N-dimethylformamide Et₂O diethyl ether EtOAc ethyl acetate EtOH ethanol LDA lithium diisopropylamide NaH sodium hydride NaHMDS sodium bis(trimethylsilyl)amide THF tetrahydrofuran

Scheme 1 describes a typical synthetic approach to the compounds of this invention. An appropriately substituted acetonitrile (X) is deprotonated by the use of a suitable base such as LDA. The resulting anion is reacted with an ester to produce an alpha-ketonitrile of formula (XI). Reaction of (XI) with thiosemicarbazide under acid catalyzed conditions results in a pyrazole of formula (XII). At this point the use of appropriate cyclization conditions, such as the use of orthoesters, yields compounds of the formula (XIII) or (XIV) or mixtures thereof. Compound (XIII) is may be converted to compound (XIV) by alkylation under basic conditions.

Compounds of formula (I) may be obtained via displacement of thioalkoxide by an amine under acidic (e.g., 1N HCl), basic (e.g., NaHMDS/THF or NaH/DMF) or neutral (e.g., 150-250° C., neat) conditions. If this reaction results in a compound where R⁴═H, it may be converted to another preferred R⁴ group in this invention using methods known to one skilled in the art of organic synthesis (for example, alkylation or reductive amination conditions).

Synthetic precursors of formula (X) in Scheme 1 may be obtained via methods known to one skilled in the art of organic synthesis. These methods include, but are not limited to, displacement of an appropriate leaving group (e.g., halide, sulfonate) by cyanide ion (as NacN or KcN), dehydration of a primary amide, or alkylation of the anion of acetonitrile with appropriate electrophiles.

If intermediates contain functional groups which are sensitive to the reaction conditions employed, these groups may be protected using methods known to those skilled in the art. These methods include, but are not limited to, those described in Protective Groups in Organic Synthesis (Greene, Wuts; 2nd ed., 1991, John Wiley & Sons, Inc.).

Other features of the invention will become apparent in the course of the following descriptions of exemplary embodiments which are given for illustration of the invention and are not intended to be limiting thereof.

EXAMPLES

Abbreviations used in the Examples are defined as follows: “1×” for once, “2×” for twice, “3×” for thrice, “° C.” for degrees Celsius, “eq” for equivalent or equivalents, “g” for gram or grams, “mg” for milligram or milligrams, “mL” for milliliter or milliliters, “¹H” for proton, “h” for hour or hours, “M” for molar, “min” for minute or minutes, “MHz” for megahertz, “MS” for mass spectroscopy, “NMR” for nuclear magnetic resonance spectroscopy, “rt” for room temperature, “tlc” for thin layer chromatography, “v/v” for volume to volume ratio. “α”, “β”, “R” and “S” are stereochemical designations familiar to those skilled in the art.

Example 1 8-(1-Ethyl)propyl-2-methyl-4-(2,4,6-trimethylphenyl)aminopyrazolo[1,5-a]triazine

Part A

To a stirring solution of sodium cyanide (1.62 g, 33 mmol) and potassium iodide (66 mg, 0.4 mmol) in dimethyl sulfoxide (20 mL) at 40° C., was slowly added 1-bromo-2-ethylbutane over 30 min. while gradually increasing the temperature to 80° C. The reaction mixture was stirred at 80° C. for 12 h, then at 110° C. for 4 h. The reaction mixture was cooled and partitioned between Et₂O and water. The organic layer was washed with brine, dried over Na₂SO₄, filtered and evaporated in vacuo to yield 2.9 g (87% yield) of 1-cyano-2-ethylbutane as an amber oil. ¹H NMR (300 mHz, CDCl₃): δ2.34 (d, 2H), 1.58(m, 1H), 1.46(m, 4H), 0.92(t, 6H).

Part B

To a stirring solution of diisopropylamine (3.72 mL, 28.35 mmol) in anhydrous THF (75 mL) at −78° C. was added 11.4 mL of a 2.5M solution of n-butyllithium in hexanes. The solution was allowed to warm to 0° C., then cooled back down to −78° C. A solution of 1-cyano-2-ethylbutane (3 g, 27 mmol) in anhydrous THF (15 mL) was added to the cooled solution. After stirring for 10 min., ethyl formate (2.7 mL, 32.4 mmol) was added and the resulting reaction mixture was stirred at −78° C. for 1 h, then allowed to slowly warm to room temperature over 3 h. The reaction mixture was then partitioned between Et₂O and water. The organic layer was washed with water and the aqueous layers were combined and acidified with 1N HCl. The resulting acidic aqueous mixture was extracted with Et₂O. The organic layer was washed with brine, dried over Na₂SO₄, filtered and evaporated in vacuo to yield a colorless oil. This residue was dissolved in ethanol (15 mL) and to the resulting solution was added water (10 mL), thiosemicarbazide (2.71 g, 29.7 mmol), and acetic acid (5.5 mL). The resulting mixture was stirred under reflux for 3 hr., then cooled and diluted with water (25 mL). The off-white precipitate which formed was collected by vacuum filtration to yield 4.7 g of the 5-amino-1-thiocarbamoylpyrazole. ¹H NMR (300 mHz, CDCl₃): δ7.2 (bs, 1H), 7.17 (d, 1H, J=4.4 Hz), 6.37 (bs, 1H), 3.65 (t, 1H, J=4.4, 4.8 Hz), 1.71 (m, 1H), 1.53 (m, 4H), 0.97 (m, 6H). Spectrum corresponds to imine tautomer. ¹H NMR (300 mHz, dmso-d₆): δ8.3 (bs, 1H), 7.4 (bs, 1H), 7.36 (d, 1H, J=4.8 Hz), 3.93 (t, 1H, J=5.13, 4.8 Hz), 1.76 (m, 1H), 1.4 (m, 4H), 0.89 (m, 6H). Spectrum corresponds to imine tautomer.

Part C

A mixture of product from Part B (1 g, 4.71 mmol) in 5 mL of trimethyl orthoacetate was refluxed for 2 h. The reaction mixture was then concentrated in vacuo to yield an amber residue. The desired cyclized product was the major component by MS (NH₃-CI).

Part D

A mixture of crude product from Part C (250 mg, 1 mmol) and trimethylaniline (0.07 mL, 0.5 mmol) in 1N HCl (1 mL) was refluxed for 1 hr. The reaction mixture was partitioned between EtOAc and 5% aq. NaHCO₃. The organic layer was dried over Na₂SO₄, filtered and evaporated in vacuo to yield a residue which was purified by column chromatography on silica gel (10%-25% EtOAc in Hexane gradient). The title compound was collected as a white solid (31 mg). ¹H NMR (300 mHz, CDCl₃): δ7.80 (s, 1H); 7.75 (s, 1H); 6.98 (s, 2H); 2.83 (m, 1H); 2.44 (s, 3H); 2.33 (s, 3H); 2.25 (s, 6H); 1.79-1.67 (m, 4H); 0.87 (t, 6H, J=7.3 Hz). MS(NH3-CI) m/z 338 (M+H)⁺. Elemental analysis: Theory (C: 71.18%, H: 8.06%, N: 20.75%); Found (C: 71.30%, H: 7.71%, N: 20.70%)

Example 2 8-(1-Ethyl)propyl-2-methyl-4-(2-chloro-4,6dimethylphenyl)aminopyrazolo[1,5-a]triazine

Part A

A mixture of product from Ex. 1, Part B (1 g, 4.71 mmol) in 5 mL of triethyl orthoacetate was refluxed for 2 h. The reaction mixture was then concentrated in vacuo to give an amber residue which was chromatographed on silica gel (100% Hexane-20% EtOAc in Hexane gradient) to yield 250 mg of cyclized product as a pale yellow oil. ¹H NMR (300 mHz, CDCl₃): δ7.91 (s, 1H); 3.35 (quart, 2H, J=7.7, 7.3, 7.3 Hz); 2.81 (m, 1H); 2.63 (s, 3H); 1.8-1.6 (m, 4H); 1.49 (t, 3H, J=7.7, 7.3 Hz); 0.81 (t, 6H, J=7.3 Hz). MS(NH₃-CI) m/z 265 (M+H)⁺.

Part B

To a solution of product from Part A (50 mg, 0.189 mmol) and 2-chloro-4,6-dimethylaniline (30 mg, 0.189 mmol) in THF (3 mL) was added 0.38 mL of 1.0M sodium bis(trimethylsilyl)amide in THF. The reaction mixture was stirred at room temperature for 30 min. The reaction mixture was then partitioned between EtOAc and water. The organic layer was dried over Na₂SO₄, filtered and evaporated in vacuo to yield a residue which was purified by column chromatography on silica gel (100% Hexane-25% EtOAc in Hexane gradient). The title compound was collected as a white solid (32 mg). MS(NH₃-CI) m/z 358 (M+H)⁺. ps Compounds in Table 1 not previously described can be made by similar procedures.

TABLE 1

Ex. R¹ R² R³ R R⁴ MS^(a) 1 CH₃ H CH(CH₂CH₃)₂ 2,4,6-Me₃Ph H 338.1 2 CH₃ H CH(CH₂CH₃)₂ 2-Cl-4,6-Me₂Ph H 358.3 3 CH₃ H CH(CH₂CH₃)₂ 2,4-Me₂Ph H 324.1 4 CH₃ H CH(CH₂CH₃)₂ 2,4-Cl₂Ph H 5 CH₃ H CH(CH₂CH₃)₂ 2-Cl-4-CF₃Ph H 6 CH₃ H CH(CH₂CH₃)₂ 2-CF₃-4-ClPh H 7 CH₃ H CH(CH₂CH₃)₂ 2,4,6-Cl₃Ph H 8 CH₃ H CH(CH₂CH₃)₂ 2,6-Me₂-4-OMePh H 9 CH₃ H CH(CH₂CH₃)₂ 2-Me-4-OMePh H 10 CH₃ H CH(CH₂CH₃)₂ 2,5-Me₂-4-OMePh H 11 CH₃ H CH(CH₂CH₃)₂ 2-Cl-4,6-Me₂-5- H F—Ph 12 CH₃ H CH(CH₂CH₃)₂ 2-OMe-4,6-Me₂Ph H 13 CH₃ H CH(CH₂CH₃)₂ 2,4-Cl₂-6-MePh H 14 CH₃ H CH(CH₂CH₃)₂ 2-OMe-4-MePh H 15 CH₃ H CH(CH₂CH₃)₂ 2-N(Me)₂-4-Me-3- H pyridyl 16 CH₃ H CH(CH₂OCH₃)Et 2,4,6-Me₃Ph H 17 CH₃ H CH(CH₂OCH₃)Et 2,4-Me₂Ph H 18 CH₃ H CH(CH₂OCH₃)Et 2-Cl-4,6-Me₂Ph H 19 CH₃ H CH(CH₂OCH₃)Et 2,4-Cl₂Ph H 20 CH₃ H CH(CH₂OCH₃)Et 2-Cl-4-CF₃Ph H 21 CH₃ H CH(CH₂OCH₃)Et 2-CF₃-4-ClPh H 22 CH₃ H CH(CH₂OCH₃)Et 2,4,6-Cl₃Ph H 23 CH₃ H CH(CH₂OCH₃)Et 2,6-Me₂-4-OMePh H 24 CH₃ H CH(CH₂OCH₃)Et 2-Me-4-OMePh H 25 CH₃ H CH(CH₂OCH₃)Et 2,5-Me₂-4-OMePh H 26 CH₃ H CH(CH₂OCH₃)Et 2-Cl-4,6-Me₂-5- H F—Ph 27 CH₃ H CH(CH₂OCH₃)Et 2-OMe-4,6-Me₂Ph H 28 CH₃ H CH(CH₂OCH₃)Et 2,4-Cl₂-6-MePh H 29 CH₃ H CH(CH₂OCH₃)Et 2-OMe-4-MePh H 30 CH₃ H CH(CH₂OCH₃)Et 2-N(Me)₂-4-Me-3- H pyridyl 31 CH₃ H CH(CH₂OCH₃)₂ 2,4,6-Me₃Ph H 370.2 32 CH₃ H CH(CH₂OCH₃)₂ 2,4-Me₂Ph H 33 CH₃ H CH(CH₂OCH₃)₂ 2-Cl-4,6-Me₂Ph H 390.1 34 CH₃ H CH(CH₂OCH₃)₂ 2,4-Cl₂Ph H 35 CH₃ H CH(CH₂OCH₃)₂ 2-Cl-4-CF₃Ph H 36 CH₃ H CH(CH₂OCH₃)₂ 2-CF₃-4-ClPh H 37 CH₃ H CH(CH₂OCH₃)₂ 2,4,6-Cl₃Ph H 38 CH₃ H CH(CH₂OCH₃)₂ 2,6-Me₂-4-OMePh H 39 CH₃ H CH(CH₂OCH₃)₂ 2-Me-4-OMePh H 40 CH₃ H CH(CH₂OCH₃)₂ 2,5-Me₂-4-OMePh H 41 CH₃ H CH(CH₂OCH₃)₂ 2-Cl-4,6-Me₂-5- H F—Ph 42 CH₃ H CH(CH₂OCH₃)₂ 2-OMe-4,6-Me₂Ph H 43 CH₃ H CH(CH₂OCH₃)₂ 2,4-Cl₂-6-MePh H 44 CH₃ H CH(CH₂OCH₃)₂ 2-OMe-4-MePh H 45 CH₃ H CH(CH₂OCH₃)₂ 2-N(Me)₂-4-Me-3- H pyridyl 46 CH₃ H CH(cPr)₂ 2,4,6-Me₃Ph H 47 CH₃ H CH(cPr)₂ 2,4-Me₂Ph H 48 CH₃ H CH(cPr)₂ 2-Cl-4,6-Me₂Ph H 49 CH₃ H CH(cPr)₂ 2,4-Cl₂Ph H 50 CH₃ H CH(cPr)₂ 2-Cl-4-CF₃Ph H 51 CH₃ H CH(cPr)₂ 2-CF₃-4-ClPh H 52 CH₃ H CH(cPr)₂ 2,4,6-Cl₃Ph H 53 CH₃ H CH(cPr)₂ 2,6-Me₂-4-OMePh H 54 CH₃ H CH(cPr)₂ 2-Me-4-OMePh H 55 CH₃ H CH(cPr)₂ 2,5-Me₂-4-OMePh H 56 CH₃ H CH(cPr)₂ 2-Cl-4,6-Me₂-5- H F—Ph 57 CH₃ H CH(cPr)₂ 2-OMe-4,6-Me₂Ph H 58 CH₃ H CH(cPr)₂ 2,4-Cl₂-6-MePh H 59 CH₃ H CH(cPr)₂ 2-OMe-4-MePh H 60 CH₃ H CH(cPr)₂ 2-N(Me)₂-4-Me-3- H pyridyl 61 CH₃ H CH(cPr)Et 2,4,6-Me₃Ph H 62 CH₃ H CH(cPr)Et 2,4-Me₂Ph H 63 CH₃ H CH(cPr)Et 2-Cl-4,6-Me₂Ph H 64 CH₃ H CH(cPr)Et 2,4-Cl₂Ph H 65 CH₃ H CH(cPr)Et 2-Cl-4-CF₃Ph H 66 CH₃ H CH(cPr)Et 2-CF₃-4-ClPh H 67 CH₃ H CH(cPr)Et 2,4,6-Cl₃Ph H 68 CH₃ H CH(cPr)Et 2,6-Me₂-4-OMePh H 69 CH₃ H CH(cPr)Et 2-Me-4-OMePh H 70 CH₃ H CH(cPr)Et 2,5-Me₂-4-OMePh H 71 CH₃ H CH(cPr)Et 2-Cl-4,6-Me₂-5- H F—Ph 72 CH₃ H CH(cPr)Et 2-OMe-4,6-Me₂Ph H 73 CH₃ H CH(cPr)Et 2,4-Cl₂-6-MePh H 74 CH₃ H CH(cPr)Et 2-OMe-4-MePh H 75 CH₃ H CH(cPr)Et 2-N(Me)₂-4-Me-3- H pyridyl 76 CH₃ H CH(cPr)Pr 2,4,6-Me₃Ph H 77 CH₃ H CH(cPr)Pr 2,4-Me₂Ph H 78 CH₃ H CH(cPr)Pr 2-Cl-4,6-Me₂Ph H 79 CH₃ H CH(cPr)Pr 2,4-Cl₂Ph H 80 CH₃ H CH(cPr)Pr 2-Cl-4-CF₃Ph H 81 CH₃ H CH(cPr)Pr 2-CF₃-4-ClPh H 82 CH₃ H CH(cPr)Pr 2,4,6-Cl₃Ph H 83 CH₃ H CH(cPr)Pr 2,6-Me₂-4-OMePh H 84 CH₃ H CH(cPr)Pr 2-Me-4-OMePh H 85 CH₃ H CH(cPr)Pr 2,5-Me₂-4-OMePh H 86 CH₃ H CH(cPr)Pr 2-Cl-4,6-Me₂-5- H F—Ph 87 CH₃ H CH(cPr)Pr 2-OMe-4,6-Me₂Ph H 88 CH₃ H CH(cPr)Pr 2,4-Cl₂-6-MePh H 89 CH₃ H CH(cPr)Pr 2-OMe-4-MePh H 90 CH₃ H CH(cPr)Pr 2-N(Me)₂-4-Me-3- H pyridyl 91 CH₃ H CH(Me)Pr 2,4,6-Me₃Ph H 92 CH₃ H CH(Me)Pr 2,4-Me₂Ph H 93 CH₃ H CH(Me)Pr 2-Cl-4,6-Me₂Ph H 94 CH₃ H CH(Me)Pr 2,4-Cl₂Ph H 95 CH₃ H CH(Me)Pr 2-Cl-4-CF₃Ph H 96 CH₃ H CH(Me)Pr 2-CF₃-4-ClPh H 97 CH₃ H CH(Me)Pr 2,4,6-Cl₃Ph H 98 CH₃ H CH(Me)Pr 2,6-Me₂-4-OMePh H 99 CH₃ H CH(Me)Pr 2-Me-4-OMePh H 100 CH₃ H CH(Me)Pr 2,5-Me₂-4-OMePh H 101 CH₃ H CH(Me)Pr 2-Cl-4,6-Me₂-5- H F—Ph 102 CH₃ H CH(Me)Pr 2-OMe-4,6-Me₂Ph H 103 CH₃ H CH(Me)Pr 2,4-Cl₂-6-MePh H 104 CH₃ H CH(Me)Pr 2-OMe-4-MePh H 105 CH₃ H CH(Me)Pr 2-N(Me)₂-4-Me-3- H pyridyl ^(a)Observed (M + H)⁺ ion under (NH₃-CI) MS conditions.

UTILITY

Compounds of this invention are expected to have utility in the treatment of inbalances associated with abnormal levels of CRF in patients suffering from depression, affective disorders, and/or anxiety.

CRF-R1 Receptor Binding Assay for the Evaluation of Biological Activity

The following is a description of the isolation of cell membranes containing cloned human CRF-R1 receptors for use in the standard binding assay as well as a description of the assay itself.

Messenger RNA was isolated from human hippocampus. The mRNA was reverse transcribed using oligo (dt) 12-18 and the coding region was amplified by PCR from start to stop codons The resulting PCR fragment was cloned into the EcoRV site of PGEMV, from whence the insert was reclaimed using XhoI+XbaI and cloned into the XhoI+XbaI sites of vector pm3ar (which contains a CMV promoter, the SV40 ‘t’ splice and early poly A signals, an Epstein-Barr viral origin of replication, and a hygromycin selectable marker). The resulting expression vector, called phchCRFR was transfected in 293EBNA cells and cells retaining the episome were selected in the presence of 400 μM hygromycin. Cells surviving 4 weeks of selection in hygromycin were pooled, adapted to growth in suspension and used to generate membranes for the binding assay described below. Individual aliquots containing approximately 1×10⁸ of the suspended cells were then centrifuged to form a pellet and frozen.

For the binding assay a frozen pellet described above containing 293EBNA cells transfected with hCRFR1 receptors is homogenized in 10 ml of ice cold tissue buffer (50 mM HEPES buffer pH 7.0, containing 10 mM MgCl₂, 2 mM EGTA, 1 μg/l aprotinin, 1 μg/ml leupeptin and 1 μg/ml pepstatin). The homogenate is centrifuged at 40,000×g for 12 min and the resulting pellet rehomogenized in 10 ml of tissue buffer. After another centrifugation at 40,000×g for 12 min, the pellet is resuspended to a protein concentration of 360 μg/ml to be used in the assay.

Binding assays are performed in 96 well plates; each well having a 300 μl capacity. To each well is added 50 μl of test drug dilutions (final concentration of drugs range from 10⁻¹⁰−10⁻⁵ M), 100 μl of ¹²⁵I-ovine-CRF (¹²⁵I-o-CRF) (final concentration 150 pM) and 150 μl of the cell homogenate described above. Plates are then allowed to incubate at room temperature for 2 hours before filtering the incubate over GF/F filters (presoaked with 0.3% polyethyleneimine) using an appropriate cell harvester. Filters are rinsed 2 times with ice cold assay buffer before removing individual filters and assessing them for radioactivity on a gamma counter.

Curves of the inhibition of ¹²⁵I-o-CRF binding to cell membranes at various dilutions of test drug are analyzed by the iterative curve fitting program LIGAND [P. J. Munson and D. Rodbard, Anal. Biochem. 107:220 (1980)], which provides Ki values for inhibition which are then used to assess biological activity.

A compound is considered to be active if it has a K_(i) value of less than about 10000 nM for the inhibition of CRF.

Inhibition of CRF-Stimulated Adenylate Cyclase Activity

Inhibition of CRF-stimulated adenylate cyclase activity can be performed as described by G. Battaglia et al. Synapse 1:572 (1987). Briefly, assays are carried out at 370° C. for 10 min in 200 ml of buffer containing 100 mM Tris-HCl (pH 7.4 at 37° C.), 10 mM MgCl₂, 0.4 mM EGTA, 0.1% BSA, 1 mM isobutylmethylxanthine (IBMX), 250 units/ml phosphocreatine kinase, 5 mM creatine phosphate, 100 mM guanosine 5′-triphosphate, 100 nM oCRF, antagonist peptides (concentration range 10⁻⁹ to ₁₀ ^(−6m)) and 0.8 mg original wet weight tissue (approximately 40-60 mg protein). Reactions are initiated by the addition of 1 mM ATP/[³²P]ATP (approximately 2-4 mCi/tube) and terminated by the addition of 100 ml of 50 mM Tris-HCL, 45 mM ATP and 2% sodium dodecyl sulfate. In order to monitor the recovery of cAMP, 1 μl of [³H]cAMP (approximately 40,000 dpm) is added to each tube prior to separation. The separation of [³²P]cAMP from [³²P]ATP is performed by sequential elution over Dowex and alumina columns.

In Vivo Biological Assay

The in vivo activity of the compounds of the present invention can be assessed using any one of the biological assays available and accepted within the art. Illustrative of these tests include the Acoustic Startle Assay, the Stair Climbing Test, and the Chronic Administration Assay. These and other models useful for the testing of compounds of the present invention have been outlined in C. W. Berridge and A. J. Dunn Brain Research Reviews 15:71 (1990). Compounds may be tested in any species of rodent or small mammal.

Dosage and Formulation

Compounds of this invention can be administered to treat these abnormalities by means that produce contact of the active agent with the agent's site of action in the body of a mammal. The compounds can be administered by any conventional means available for use in conjunction with pharmaceuticals either as individual therapeutic agent or in combination of therapeutic agents. They can be administered alone, but will generally be administered with a pharmaceutical carrier selected on the basis of the chosen route of administration and standard pharmaceutical practice.

The dosage administered will vary depending on the use and known factors such as pharmacodynamic character of the particular agent, and its mode and route of administration; the recipient's age, weight, and health; nature and extent of symptoms; kind of concurrent treatment; frequency of treatment; and desired effect. For use in the treatment of said diseases or conditions, the compounds of this invention can be orally administered daily at a dosage of the active ingredient of 0.002 to 200 mg/kg of body weight. Ordinarily, a dose of 0.01 to 10 mg/kg in divided doses one to four times a day, or in sustained release formulation will be effective in obtaining the desired pharmacological effect.

Dosage forms (compositions) suitable for administration contain from about 1 mg to about 100 mg of active ingredient per unit. In these pharmaceutical compositions, the active ingredient will ordinarily be present in an amount of about 0.5 to 95% by weight based on the total weight of the composition.

The active ingredient can be administered orally is solid dosage forms, such as capsules, tablets and powders; or in liquid forms such as elixirs, syrups, and/or suspensions. The compounds of this invention can also be administered parenterally in sterile liquid dose formulations.

Gelatin capsules can be used to contain the active ingredient and a suitable carrier such as but not limited to lactose, starch, magnesium stearate, steric acid, or cellulose derivatives. Similar diluents can be used to make compressed tablets. Both tablets and capsules can be manufactured as sustained release products to provide for continuous release of medication over a period of time. Compressed tablets can be sugar-coated or film-coated to mask any unpleasant taste, or used to protect the active ingredients from the atmosphere, or to allow selective disintegration of the tablet in the gastrointestinal tract.

Liquid dose forms for oral administration can contain coloring or flavoring agents to increase patient acceptance.

In general, water, pharmaceutically acceptable oils, saline, aqueous dextrose (glucose), and related sugar solutions and glycols, such as propylene glycol or polyethylene glycol, are suitable carriers for parenteral solutions. Solutions for parenteral administration preferably contain a water soluble salt of the active ingredient, suitable stabilizing agents, and if necessary, butter substances. Antioxidizing agents, such as sodium bisulfite, sodium sulfite, or ascorbic acid, either alone or in combination, are suitable stabilizing agents. Also used are citric acid and its salts, and EDTA. In addition, parenteral solutions can contain preservatives such as benzalkonium chloride, methyl- or propyl-paraben, and chlorobutanol.

Suitable pharmaceutical carriers are described in “Remington's Pharmaceutical Sciences”, A. Osol, a standard reference in the field.

Useful pharmaceutical dosage-forms for administration of the compounds of this invention can be illustrated as follows:

Capsules

A large number of units capsules are prepared by filling standard two-piece hard gelatin capsules each with 100 mg of powdered active ingredient, 150 mg lactose, 50 mg cellulose, and 6 mg magnesium stearate.

Soft Gelatin Capsules

A mixture of active ingredient in a digestible oil such as soybean, cottonseed oil, or olive oil is prepared and injected by means of a positive displacement was pumped into gelatin to form soft gelatin capsules containing 100 mg of the active ingredient. The capsules were washed and dried.

Tablets

A large number of tablets are prepared by conventional procedures so that the dosage unit was 100 mg active ingredient, 0.2 mg of colloidal silicon dioxide, 5 mg of magnesium stearate, 275 mg of microcrystalline cellulose, 11 mg of starch, and 98.8 mg lactose. Appropriate coatings may be applied to increase palatability or delayed adsorption.

The compounds of this invention may also be used as reagents or standards in the biochemical study of neurological function, dysfunction, and disease.

Obviously, numerous modifications and variations of the present invention are possible in light of the above teachings. It is therefore to be understood that within the scope of the appended claims, the invention may be practiced otherwise that as specifically described herein. 

What is claimed as new and desired to be secured by Letter Patent of United States is:
 1. A compound of formula (I):

wherein; X is selected from N, CH and CR⁵; R¹ is selected from H, C₁₋₄ alkyl, C₂₋₄ alkenyl, C₂₋₄ alkynyl, Cl, F, Br, I, —CN, C₁₋₄ haloalkyl, NH₂, NH(CH₃), N(CH₃)₂, NHC(O)CH₃, N(CH₃)C(O)CH₃, OH, C₁₋₄ alkoxy, SH, SCH₃, S(O)CH₃, and S(O)₂CH₃; R² is selected from H, C₁₋₄ alkyl, C₃₋₆ cycloalkyl, Cl, F, Br, I, C₁₋₄ haloalkyl, —CN, NH(CH₃), N(CH₃)₂, NHC(O)CH₃, N(CH₃)C(O)CH₃, OH, C₁₋₄ alkoxy, SH, SCH₃, S(O)CH₃, and S(O)₂CH₃; R³ is selected from C₁₋₁₀ alkyl substituted with 0-3 R^(a), C₂₋₁₀ alkenyl substituted with 0-3 R^(a), C₂₋₁₀ alkynyl substituted with 0-3 R^(a), C₃₋₈ cycloalkyl substituted with 0-3 R^(a), and (C₃₋₆ cycloalkyl)C₁₋₄ alkyl substituted with 0-3 R^(a); R^(a) is independently selected at each occurrence from ═O, C₁₋₆ alkyl, C₃₋₆ cycloalkyl, Cl, F, Br, I, C₁₋₄ haloalkyl, —CN, —OR^(10a), SH, —S(O)_(n)R¹², —COR¹³, —C(O)OR¹³, —OC(O)R¹⁴, —NR⁸COR¹³, —NR⁸CONR⁶R⁷, —NR⁸C(O)OR¹², —NR⁶R⁷, —CONR⁶R⁷, aryl, heteroaryl and heterocyclyl; R⁴ is selected from H, C₁₋₄ alkyl substituted with 0-1 R^(b), allyl substituted with 0-1 R^(c), and propargyl substituted with 0-1 R^(c); R^(b) is selected from C₃₋₆ cycloalkyl, —NR⁶R⁷, —OR¹⁰, —S(O)_(n)R¹¹ and —C(O)OR¹³; R^(c) is selected from C₁₋₄ alkyl and C₃₋₆ cycloalkyl; R⁵ is independently selected at each occurrence from C₁₋₆ alkyl substituted with 0-2 R^(d), C₂₋₆ alkenyl substituted with 0-2 R^(d), C₂₋₆ alkynyl substituted with 0-2 R^(d), C₃₋₆ cycloalkyl substituted with 0-2 R^(d), (C₃₋₆ cycloalkyl)C₁₋₄ alkyl substituted with 0-2 R^(d), —NO₂, Cl, F, Br, I, —CN, C₁₋₄ haloalkyl, —NR⁶R⁷, —NR⁸COR¹³, —NR⁸C(O) OR¹², —COR¹³, —OR¹⁰, —CONR⁶R⁷, —NR⁸CONR⁶R⁷, —C(O)OR¹⁰, SH, and —S(O)_(n)R¹²; R^(d) is independently selected at each occurrence from C₁₋₄ alkyl, —NO₂, Cl, F, Br, I, —CN, —NR⁶R⁷, —NR⁸COR¹³, —NR⁸C(O)OR¹², —COR¹³, —OR¹⁰, —CONR⁶R⁷, —NR⁸CONR⁶R⁷, —C(O)OR¹⁰, SH, and —S(O)_(n)R¹²; R⁶ is independently selected at each occurrence from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)methyl, and C₁₋₄ haloalkyl; R⁷ is independently selected at each occurrence from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)methyl, and C₁₋₄ haloalkyl; alternatively, NR⁶R⁷ is selected from piperidine, pyrrolidine, morphbline, thiomorpholine, thiomorpholine-oxide, and thiomorpholine-dioxide, and is substituted with 0-1 R^(e); R^(e) is C₁₋₄ alkyl; alternatively, NR⁶R⁷ is piperazine substituted on the nitrogen with 0-1 R^(f) and substituted on a carbon with 0-1 R^(e); R^(f) is selected from C₁₋₄ alkyl, C(O)C₁₋₄ alkyl, C(O)benzyl, C(O)OC₁₋₄ alkyl, C(O)O-benzyl, SO₂—C₁₋₄ alkyl, SO₂-benzyl, and SO₂-phenyl; R⁸ is independently at each occurrence selected from H, C₁₋₄ alkyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, and benzyl; R¹⁰ is independently selected at each occurrence from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, C₁₋₄ hydroxyalkyl, C₁₋₄ haloalkyl, (NR⁶R⁷)C₁₋₄ alkyl, (C₁₋₄ alkyl)₂-amino-C₁₋₄ alkyl, and SO₂—C₁₋₄ alkyl; R^(10a) is independently selected at each occurrence from H, C₁₋₆ alkyl, C₂₋₄ alkenyl, phenyl, benzyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, and C₁₋₄ haloalkyl; R¹¹ is independently at each occurrence selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl, and C₃₋₆ cycloalkyl; R¹² is independently at each occurrence selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, aryl, and (aryl)C₁₋₄ alkyl; R¹³ is independently at each occurrence selected from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, and (C₃₋₆ cycloalkyl)C₁₋₄ alkyl; R¹⁴ is independently at each occurrence selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, aryl, and (aryl)C₁₋₄ alkyl; aryl is independently at each occurrence selected from phenyl and naphthyl, and is substituted with 0-3 R^(g); R^(g) is independently at each occurrence selected from C₁₋₆ alkyl, C₃₋₆ cycloalkyl, Cl, F, Br, I, C₁₋₄ haloalkyl, cyano, nitro, —OR¹⁰, SH, —S(O)_(n)R¹⁵, —COR¹⁶, —C(O)OR¹⁶, —OC(O)R¹⁷, —NR⁸COR¹⁶, —NR⁸CONR⁶R⁷, —NR⁸C(O)OR¹², —NR⁶R⁷, and —CONR⁶R⁷; R¹⁵ is independently at each occurrence selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, phenyl, benzyl, and (phenyl)C₁₋₄ alkyl; R¹⁶ is independently at each occurrence selected from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, and (C₃₋₆ cycloalkyl)C₁₋₄ alkyl; R¹⁷ is independently at each occurrence selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, phenyl, benzyl, (phenyl)C₁₋₄ alkyl, heteroaryl and (heteroaryl)C₁₋₄ alkyl; heteroaryl is independently at each occurrence selected from pyridyl, pyrimidinyl, triazinyl, furanyl, quinolinyl, isoquinolinyl, thienyl, imidazolyl, thiazolyl, indolyl, pyrrolyl, oxazolyl, benzofuranyl, benzothienyl, benzthiazolyl, isoxazolyl, pyrazolyl, triazolyl, tetrazolyl, and indazolyl, and is substituted with 0-3 R^(h); heterocyclyl is saturated or partially saturated heteroaryl, substituted with 0-3 R^(h); and R^(h) is independently at each occurrence selected from C₁₋₆ alkyl, C₃₋₆ cycloalkyl, Cl, F, Br, I, C₁₋₄ haloalkyl, cyano, nitro, —OR¹⁰, SH, —S(O)_(n)R^(l5), —COR¹⁶, —C(O)OR¹⁶, —OC(O)R¹⁸, —NR⁸COR¹⁶, —NR⁸CONR⁶R⁷, —NR⁸C(O)OR¹², —NR⁶R⁷, and —CONR⁶R⁷; R¹⁸ is independently selected at each occurrence from C₁₋₆ alkyl, C₃₋₆ cycloalkyl, phenyl and benzyl; n is independently at each occurrence selected from 0, 1 and 2; and, r is selected from 0, 1, 2, 3, and
 4. 2. A compound according to claim 1, wherein: R¹ is selected from H, CH₃, CH₂CH₃, Cl, F, Br, —CN, CF₃, NH₂, NH(CH₃), N(CH₃)₂, OH, OCH₃, SH, SCH₃, and S(O)₂CH₃; R² is selected from H, CH₃, CH₂CH₃, Cl, F, Br, —CN, CF₃, NH(CH₃), N(CH₃)₂, OH, OCH₃, SH, SCH₃, and S(O)₂CH₃; R³ is selected from C₁₋₆ alkyl substituted with 0-2 R^(a), C₂₋₆ alkenyl substituted with 0-2 R^(a), and C₂₋₆ alkynyl substituted with 0-2 R^(a); R^(a) is independently selected at each occurrence from ═O, CH₃, CH₂CH₃, cyclopropyl, cyclopentyl, cyclohexyl, Cl, F, Br, CF₃, —CN, —OH, OHC₃, OCH₂CH₃, SH, —S(O)_(n)R¹², —COR¹³, —C(O)OR¹³, —NR⁸COR¹³, —NR⁶R⁷, —CONR⁶R⁷, aryl, heteroaryl and heterocyclyl; R⁴ is selected from H, CH₃, CH₂CH₃; R⁵ is independently selected at each occurrence from CH₃, CH₂CH₃, cyclopropyl, cyclopentyl, cyclohexyl, Cl, F, Br, —CN, CF₃, —NR⁶R⁷, COR¹³, —OR¹⁰, —CONR⁶R⁷, —C(O)OR¹⁰, SH, and —S(O)_(n)R¹²; R⁶ is independently selected at each occurrence from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)methyl, and C₁₋₄ haloalkyl; R⁷ is independently selected at each occurrence from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)methyl, and C₁₋₄ haloalkyl; alternatively, NR⁶R⁷ is selected from piperidine, pyrrolidine, morpholine, thiomorphollne, thiomorpholine-oxide, and thiomorpholine-dioxide, and is substituted with 0-1 R^(e); R^(e) is CH₃; alternatively, NR⁶R⁷ is piperazine substituted on the nitrogen with 0-1 R^(f) and substituted on a carbon with 0-1 R^(e); R^(f) is selected from CH₃, C(O)CH₃, C(O)benzyl, C₂CH₃, CO₂-benzyl, SO₂CH₃, SO₂-benzyl, and SO₂-phenyl; R⁸ is independently at each occurrence selected from H and C₁₋₄ alkyl; R¹⁰ is independently selected at each occurrence from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, C₁₋₄ hydroxyalkyl, C₁₋₄ haloalkyl, (NR⁶R⁷)C₁₋₄ alkyl, (C₁₋₄ alkyl)₂-amino-C₁₋₄ alkyl, and SO₂—C₁₋₄ alkyl; R¹² is independently at each occurrence selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, aryl, and (aryl)C₁₋₄ alkyl; p1 R¹³ is independently at each occurrence selected from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, and (C₃₋₆ cycloalkyl)C₁₋₄ alkyl; aryl is independently at each occurrence selected from phenyl and naphthyl, and is substituted with 0-3 R^(g); R^(g) is independently at each occurrence selected from C₁₋₆ alkyl, C₃₋₆ cycloalkyl, Cl, F, Br, I, C₁₋₄ haloalkyl, cyano, nitro, —OR¹⁰, SH, —S(O)_(n)R¹⁵, —COR¹⁶, —C(O)OR¹⁶, —OC(O)R¹⁷, —NR⁸COR¹⁶, —NR⁸CONR⁶R⁷, —NR⁸C(O)OR¹², —NR⁶R⁷, and —CONR⁶R⁷; R¹⁵ is independently at each occurrence selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, phenyl, benzyl, and (phenyl)C₁₋₄ alkyl; R¹⁶ is independently at each occurrence selected from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, and (C₃₋₆ cycloalkyl)C₁₋₄ alkyl; R¹⁷ is independently at each occurrence selected from C₁₋₄ alkyl, C₁₋₄ haloalkyl, (C₁₋₄ alkoxy)C₁₋₄ alkyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)C₁₋₄ alkyl, phenyl, benzyl, (phenyl)C₁₋₄ alkyl, heteroaryl and (heteroaryl)C₁₋₄ alkyl; heteroaryl is independently at each occurrence selected from pyridyl, pyrimidinyl, triazinyl, furanyl, quinolinyl, isoquinolinyl, thienyl, imidazolyl, thiazolyl, indolyl, pyrrolyl, oxazolyl, benzofuranyl, benzothienyl, benzthiazolyl, isoxazolyl, pyrazolyl, triazolyl, tetrazolyl, and indazolyl, and is substituted with 0-3 R^(h); heterocyclyl is saturated or partially saturated heteroaryl, substituted with 0-3 R^(h); and R^(h) is independently at each occurrence selected from CH₃, CH₂CH₃, cyclopropyl, cyclopentyl, cyclohexyl, Cl, F, Br, CF₃, —CN, nitro, —OR¹⁰, SH, —S(O)_(n)R¹⁵, —COR¹⁶, —C(O)OR¹⁶, —NR⁶R⁷, and —CONR⁶R⁷; n is independently at each occurrence selected from 0, 1 and 2; and, r is selected from 0, 1, 2, 3, and
 4. 3. A compound according to claim 2, wherein: R¹ is selected from H, CH₃, CH₂CH₃, Cl, and F; R² is selected from H, CH₃, CH₂CH₃, Cl and F; R³ is selected from C₁₋₆ alkyl substituted with 0-2 R^(a), C₂₋₆ alkenyl substituted with 0-2 R^(a), and C₂₋₆ alkynyl substituted with 0-2 R^(a); R^(a) is independently selected at each occurrence from CH₃, CH₂CH₃, cyclopropyl, cyclopentyl, cyclohexyl, Cl, F, Br, CF₃, —CN, —OH, OCH₃, and OCH₂CH₃; R⁴ is selected from H, CH₃, CH₂CH₃; R⁵ is independently selected at each occurrence from CH₃, CH₂CH₃, CH(CH₃)₂, cyclopropyl, cyclopentyl, cyclohexyl, Cl, F, Br, —CN, CF₃, —NR⁶R⁷, OCH₃, OCH₂CH₃, SCH₃, SOCH₃, and SO₂CH₃; R⁶ is independently selected at each occurrence from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)methyl, and C₁₋₄ haloalkyl; R⁷ is independently selected at each occurrence from H, C₁₋₆ alkyl, phenyl, benzyl, C₃₋₆ cycloalkyl, (C₃₋₆ cycloalkyl)methyl, and C₁₋₄ haloalkyl; alternatively, NR⁶R⁷ is selected from piperidine, pyrrolidine, morpholine, thiomorpholine, thiomorpholine-oxide, and thiomorpholine-dioxide, and is substituted with 0-1 R^(e); R^(e) is CH₃; alternatively, NR⁶R⁷ is piperazine substituted on the nitrogen with 0-1 R^(f) and substituted on a carbon with 0-1 R^(e); R^(f) is selected from CH₃, CH₂CH₃, C(O)CH₃, CO₂CH₃, SO₂CH₃, and CO₂-benzyl; and, r is selected from 1, 2, and
 3. 4. A compound according to claim 3, wherein: R¹ is CH₃; R² is selected from H and CH₃; R³ is selected from 2-propyl, 2-butyl, 2-pentyl, 3-pentyl, trans-pent-2-en-4-yl, pent-2-yn-4-yl, 3-hexyl, hex-1-en-3-yl, hex-2-yn-4-yl, 1-(cyclopropyl)ethyl, 1-(cyclopropyl)propyl, 3-(cyclopropyl)prop-1-en-3-yl, 1-(cyclopropyl)butyl, dicyclopropylmethyl, 1-(cyclopropyl)but-2-yn-1-yl, trans-1-(cyclopropyl)but-2-en-1-yl, 1-(cyclobutyl)ethyl, 1-(cyclobutyl)propyl, 1-(cyclobutyl)butyl, 1-(cyclopropyl)but-2-yn-1-yl, dicyclobutylmethyl, cyclopentyl, 1-methoxyprop-2-yl, 1-methoxybut-2-yl, 1,3-dimethoxyprop-2-yl, 1,4-dimethoxybut-2-yl, and 1-cyclopropyl-2-methoxyethyl; R⁴ is selected from H, CH₃, and CH₂CH₃; R⁵ is independently selected at each occurrence from CH₃, CH₂CH₃, CH(CH₃)₂, cyclopropyl, cyclopentyl, cyclohexyl, Cl, F, Br, —CN, CF₃, —NR⁶R⁷, OCH₃, OCH₂CH₃, SCH₃, SOCH₃, and SO₂CH₃; R⁶ is independently selected at each occurrence from H, CH₃, CH₂CH₃, phenyl, benzyl, cyclopropyl, cyclopentyl, cyclohexyl, cyclopropylmethyl, cyclopentylmethyl, cyclohexylmethyl, and CF₃; R⁷ is independently selected at each occurrence from H, CH₃, CH₂CH₃, phenyl, benzyl, cyclopropyl, cyclopentyl, cyclohexyl, cyclopropylmethyl, cyclopentylmethyl, cyclohexylmethyl, and CF₃; alternatively, NR⁶R⁷ is selected from piperidine, pyrrolidine, morpholine, thiomorpholine, thiomorpholine-oxide, and thiomorpholine-dioxide, and is substituted with 0-1 R^(e); R^(e) is CH₃; alternatively, NR⁶R⁷ is piperazine substituted on the nitrogen with 0-1 R^(f) and substituted on a carbon with 0-1 R^(e); R^(f) is selected from CH₃, CH₂CH₃, C(O)CH₃, CO₂CH₃, SO₂CH₃, and C₂-benzyl; and, r is selected from 1, 2, and
 3. 5. A compound according to claim 1, wherein the compound is selected from the group: 8-(3-Pentyl)-2-methyl-4-(2,4,6-trimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(3-Pentyl)-2-methyl-4-(2-chloro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(3-Pentyl)-2-methyl-4-(4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(3-Pentyl)-2-methyl-4-(2,4-dichlorophenyl)aminopyrazolo[1,5-a]triazine; 8-(3-Pentyl)-2-methyl-4-(2-chloro-4-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(3-Pentyl)-2-methyl-4-(4-chloro-2-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(3-Pentyl)-2-methyl-4-(2,4,6-trichlorophenyl)aminopyrazolo[1,5-a]triazine; 8-(3-Pentyl)-2-methyl-4-(2,6-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(3-Pentyl)-2-methyl-4-(2-methyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(3-Pentyl)-2-methyl-4-(2,5-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(3-Pentyl)-2-methyl-4-(2-chloro-5-fluoro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(3-Pentyl)-2-methyl-4-(4,6-dimethyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(3-Pentyl)-2-methyl-4-(2,4-dichloro-6-methylphenyl)aminopyrazolo[1,5-a]triazine; 8-(3-Pentyl)-2-methyl-4-(4-methyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine; or a pharmaceutically acceptable salt form thereof.
 6. A pharmaceutical composition, comprising: a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound according to claim 1, or a pharmaceutically acceptable salt form thereof.
 7. A compound according to claim 1, wherein the compound is selected from the group: 8-(1-Methoxybut-2-yl)-2-methyl-4-(2,4,6-trimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Methoxybut-2-yl)-2-methyl-4-(2-chloro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Methoxybut-2-yl)-2-methyl-4-(4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Methoxybut-2-yl)-2-methyl-4-(2,4-dichlorophenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Methoxybut-2-yl)-2-methyl-4-(2-chloro-4-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Methoxybut-2-yl)-2-methyl-4-(4-chloro-2-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Methoxybut-2-yl)-2-methyl-4-(2,4,6-trichlorophenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Methoxybut-2-yl)-2-methyl-4-(2,6-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Methoxybut-2-yl)-2-methyl-4-(2-methyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Methoxybut-2-yl)-2-methyl-4-(2,5-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Methoxybut-2-yl)-2-methyl-4-(2-chloro-5-fluoro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Methoxybut-2-yl)-2-methyl-4-(4,6-dimethyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Methoxybut-2-yl)-2-methyl-4-(2,4-dichloro-6-methylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Methoxybut-2-yl)-2-methyl-4-(4-methyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine; or a pharmaceutically acceptable salt form thereof.
 8. A compound according to claim 1, wherein the compound is selected from the group 8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2,4,6-trimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2-chloro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2,4-dichlorophenyl)aminopyrazolo[1,5-a]triazine; 8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2-chloro-4-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(4-chloro-2-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2,4,6-trichlorophenyl)aminopyrazolo[1,5-a]triazine; 8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2,6-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2-methyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2,5-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2-chloro-5-fluoro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(4,6-dimethyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2,4-dichloro-6-methylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(4-methyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine; or a pharmaceutically acceptable salt form thereof.
 9. A compound according to claim 1, wherein the compound is selected from the group: 8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2,4,6-trimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2-chloro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2,4-dichlorophenyl)aminopyrazolo[1,5-a]triazine; 8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2-chloro-4-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(4-chloro-2-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2,4,6-trichlorophenyl)aminopyrazolo[1,5-a]triazine; 8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2,6-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2-methyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2,5-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2-chloro-5-fluoro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(4,6-dimethyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2,4-dichloro-6-methylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(4-methyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine; or a pharmaceutically acceptable salt form thereof.
 10. A compound according to claim 1, wherein the compound is selected from the group: 8-(1-Cyclopropyl)propyl-2-methyl-4-(2,4,6-trimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)propyl-2-methyl-4-(2-chloro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)propyl-2-methyl-4-(4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)propyl-2-methyl-4-(2,4-dichlorophenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)propyl-2-methyl-4-(2-chloro-4-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)propyl-2-methyl-4-(4-chloro-2-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)propyl-2-methyl-4-(2,4,6-trichlorophenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)propyl-2-methyl-4-(2,6-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)propyl-2-methyl-4-(2-methyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)propyl-2-methyl-4-(2,5-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)propyl-2-methyl-4-(2-chloro-5-fluoro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)propyl-2-methyl-4-(4,6-dimethyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)propyl-2-methyl-4-(2,4-dichloro-6-methylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)propyl-2-methyl-4-(4-methyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine; or a pharmaceutically acceptable salt form thereof.
 11. A compound according to claim 1, wherein the compound is selected from the group: 8-(1-Cyclopropyl)butyl-2-methyl-4-(2,4,6-trimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)butyl-2-methyl-4-(2-chloro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)butyl-2-methyl-4-(4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)butyl-2-methyl-4-(2,4-dichlorophenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)butyl-2-methyl-4-(2-chloro-4-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)butyl-2-methyl-4-(4-chloro-2-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)butyl-2-methyl-4-(2,4,6-trichlorophenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)butyl-2-methyl-4-(2,6-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)butyl-2-methyl-4-(2-methyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)butyl-2-methyl-4-(2,5-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)butyl-2-methyl-4-(2-chloro-5-fluoro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)butyl-2-methyl-4-(4,6-dimethyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)butyl-2-methyl-4-(2,4-dichloro-6-methylphenyl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)butyl-2-methyl-4-(4-methyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine; or a pharmaceutically acceptable salt form thereof.
 12. A compound according to claim 1, wherein the compound is selected from the group: 8-(2-Pentyl)-2-methyl-4-(2,4,6-trimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(2-Pentyl)-2-methyl-4-(2-chloro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(2-Pentyl)-2-methyl-4-(4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(2-Pentyl)-2-methyl-4-(2,4-dichlorophenyl)aminopyrazolo[1,5-a]triazine; 8-(2-Pentyl)-2-methyl-4-(2-chloro-4-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(2-Pentyl)-2-methyl-4-(4-chloro-2-trifluoromethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(2-Pentyl)-2-methyl-4-(2,4,6-trichlorophenyl)aminopyrazolo[1,5-a]triazine; 8-(2-Pentyl)-2-methyl-4-(2,6-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(2-Pentyl)-2-methyl-4-(2-methyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(2-Pentyl)-2-methyl-4-(2,5-dimethyl-4-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(2-Pentyl)-2-methyl-4-(2-chloro-5-fluoro-4,6-dimethylphenyl)aminopyrazolo[1,5-a]triazine; 8-(2-Pentyl)-2-methyl-4-(4,6-dimethyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine; 8-(2-Pentyl)-2-methyl-4-(2,4-dichloro-6-methylphenyl)aminopyrazolo[1,5-a]triazine; 8-(2-Pentyl)-2-methyl-4-(4-methyl-2-methoxyphenyl)aminopyrazolo[1,5-a]triazine; or a pharmaceutically acceptable salt form thereof.
 13. A compound according to claim 1, wherein the compound is selected from the group: 8-(3-Pentyl)-2-methyl-4-(2-dimethylamino-4-methylpyrid-3-yl)aminopyrazolo[1,5-a]triazine; 8-(1-Methoxybut-2-yl)-2-methyl-4-(2-dimethylamino-4-methylpyrid-3-yl)aminopyrazolo[1,5-a]triazine; 8-(1,3-Dimethoxyprop-2-yl)-2-methyl-4-(2-dimethylamino-4-methylpyrid-3-yl)aminopyrazolo[1,5-a]triazine; 8-(1,1-Dicyclopropyl)methyl-2-methyl-4-(2-dimethylamino-4-methylpyrid-3-yl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)propyl-2-methyl-4-(2-dimethylamino-4-methylpyrid-3-yl)aminopyrazolo[1,5-a]triazine; 8-(1-Cyclopropyl)butyl-2-methyl-4-(2-dimethylamino-4-methylpyrid-3-yl)aminopyrazolo[1,5-a]triazine; 8-(2-Pentyl)-2-methyl-4-(2-dimethylamino-4-methylpyrid-3-yl)aminopyrazolo[1,5-a]triazine, or a pharmaceutically acceptable salt form thereof.
 14. A method of treating anxiety inca mammal comprising: administering to the mammal a therapeutically effective amount of a compound of any one of claims 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12 or 13, or a pharmaceutically acceptable salt form thereof.
 15. A method of treating depression in a mammal comprising: administering to the mammal a therapeutically effective amount of a compound of any one of claims 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, or 13, or a pharmaceutically acceptable salt form thereof. 